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Carbide initiation

The third control is by use of a fixed burnable poison. This consists of rods containing a mixture of aluminum oxide and boron carbide, included in the initial fuel loading using the vacant spaces in some of the fuel assembhes that do not have control clusters. The burnable poison is consumed during operation, causing a reactivity increase that helps counteract the drop owing to fuel consumption. It also reduces the need for excessive initial soluble boron. Other reactors use gadolinium as burnable poison, sometimes mixed with the fuel. [Pg.217]

Once initiated, zirconium and carbon powders react exothermically in a vacuum or inert atmosphere to form zirconium carbide. With the greater availabiHty of relatively pure metal powders, this technique is coming into common use for the production of several refractory carbides. Zirconium carbide is not a fixed stoichiometric compound, but a defect compound with a single-phase composition ranging from ZrCQ to ZrCQ at 2400°C. [Pg.433]

Stacking faults thereby providing barriers to sHp. If carbides are allowed to precipitate to the point of becoming continuous along the grain boundaries, they often initiate fracture (see Fracture mechanics). A thorough discussion of the mechanical properties of cobalt alloys is given in References 29 and 30 (see also Refractories). [Pg.373]

Random copolymers of vinyl chloride and other monomers are important commercially. Most of these materials are produced by suspension or emulsion polymerization using free-radical initiators. Important producers for vinyl chloride—vinyUdene chloride copolymers include Borden, Inc. and Dow. These copolymers are used in specialized coatings appHcations because of their enhanced solubiUty and as extender resins in plastisols where rapid fusion is required (72). Another important class of materials are the vinyl chloride—vinyl acetate copolymers. Principal producers include Borden Chemicals Plastics, B. F. Goodrich Chemical, and Union Carbide. The copolymerization of vinyl chloride with vinyl acetate yields a material with improved processabihty compared with vinyl chloride homopolymer. However, the physical and chemical properties of the copolymers are different from those of the homopolymer PVC. Generally, as the vinyl acetate content increases, the resin solubiUty in ketone and ester solvents and its susceptibiUty to chemical attack increase, the resin viscosity and heat distortion temperature decrease, and the tensile strength and flexibiUty increase slightly. [Pg.185]

For many years use of this material was largely confined to America and it was seldom met in Europe because of the cheaper EVA materials available. In 1980, however, BP initiated production of such materials, whilst in the United States the material is produced by Union Carbide. The Dow company, whose product Zetafin was the most well-known grade, no longer supply the copolymer. [Pg.277]

This polymer first appeared commercially in 1965 (Parylene N Union Carbide). It is prepared by a sequence of reactions initiated by the pyrolysis of p-xylene at 950°C in the presence of steam to give the cyclic dimer. This, when pyrolysed at 550°C, yields monomeric p-xylylene. When the vapour of the monomer condenses on a cool surface it polymerises and the polymer may be stripped off as a free film. This is claimed to have a service life of 10 years at 220°C, and the main interest in it is as a dielectric film. A monochloro-substituted polymer (Parylene C) is also available. With both Parylene materials the polymers have molecular weights of the order of 500 000. [Pg.586]

The chains of hollow carbon may be initially chains consisting of Ni (or carbide) particles covered with graphitic carbon. The chains lying on the hot surface of the cathode are heated, and Ni atoms evaporate through defects of the outer graphitic carbon because the vapor pressure of Ni is much higher than carbon. Thus, the carbon left forms hollow graphitic layers. [Pg.159]

The companion of insert bits cutting structure is shown in Figure 4-142 [44]. Initially, the tungsten carbide tooth bit was developed to drill extremely hard, abrasive cherts and quartzites that had been very costly to drill because of the... [Pg.776]


See other pages where Carbide initiation is mentioned: [Pg.73]    [Pg.75]    [Pg.77]    [Pg.1]    [Pg.73]    [Pg.75]    [Pg.77]    [Pg.1]    [Pg.15]    [Pg.278]    [Pg.279]    [Pg.582]    [Pg.76]    [Pg.101]    [Pg.376]    [Pg.379]    [Pg.380]    [Pg.134]    [Pg.202]    [Pg.56]    [Pg.199]    [Pg.200]    [Pg.206]    [Pg.208]    [Pg.211]    [Pg.282]    [Pg.285]    [Pg.383]    [Pg.443]    [Pg.443]    [Pg.445]    [Pg.449]    [Pg.450]    [Pg.458]    [Pg.6]    [Pg.2464]    [Pg.216]    [Pg.247]    [Pg.303]    [Pg.761]    [Pg.700]    [Pg.740]    [Pg.815]    [Pg.835]    [Pg.174]    [Pg.431]    [Pg.330]   
See also in sourсe #XX -- [ Pg.557 ]




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Carbide chain initiation

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